WormBase Tree Display for DO_term: DOID:0111269
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| DOID:0111269 | Name | autosomal dominant hyaline body myopathy | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A hyaline body myopathy that has_material_basis_in heterozygous mutation in MYH7 on 14q11.2. | ||||
| Synonym | Exact | MSMA | |||
| Myopathy, myosin storage, autosomal dominant | |||||
| congenital myopathy 7A | |||||
| myopathy with lysis of type I myofibrils | |||||
| Parent | Is_a | DOID:0050736 | |||
| DOID:0111267 | |||||
| DB_info | Database | OMIM | disease | 608358 | |
| Attribute_of | Gene_by_orthology | WBGene00002348 | |||
| WBGene00003514 | |||||
| WBGene00003515 | |||||
| WBGene00006789 | |||||
| WBGene00009730 | |||||
| WBGene00019064 |
